A common VWF exon 28 haplotype in the Turkish population

Clinical and Applied Thrombosis/Hemostasis

Volumn 19, Issue 5, 2013, Pages 550-556

  Berber, Ergul ^a   Pehlevan, Funda ^b   Akin, Mehmet ^c   Capan, Ozlem Yalcin ^a,d   Kavakli, Kaan ^c   Çaglayan, S Hande ^d  

^a ISTANBUL AREL UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

^c EGE UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^d BOGAZICI UNIVERSITY   (Turkey)

Author keywords

VWD; VWF; VWF exon 28; VWF gene conversion; VWF haplotype

Indexed keywords

VON WILLEBRAND FACTOR;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; DNA DETERMINATION; DNA SEQUENCE; EXON; FAMILY ASSESSMENT; GENE CONVERSION; GENETIC ASSOCIATION; HAPLOTYPE; HETEROZYGOTE; HUMAN; POPULATION GENETICS; PRESCHOOL CHILD; PRIORITY JOURNAL; PSEUDOGENE; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TURKEY (REPUBLIC); VON WILLEBRAND DISEASE;

VWD; VWF; VWF EXON 28; VWF GENE CONVERSION; VWF HAPLOTYPE;

BASE SEQUENCE; EXONS; FEMALE; HAPLOTYPES; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; TURKEY; VON WILLEBRAND DISEASES; VON WILLEBRAND FACTOR;

EID: 84884237964     PISSN: 10760296     EISSN: 19382723     Source Type: Journal    
DOI: 10.1177/1076029612441054     Document Type: Article

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